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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 7-95592889-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=95592889&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 95592889,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_002612.4",
"consequences": [
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "NM_002612.4",
"protein_id": "NP_002603.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 411,
"cds_start": 400,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 623,
"cdna_end": null,
"cdna_length": 3601,
"mane_select": "ENST00000005178.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_002612.4"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000005178.6",
"protein_id": "ENSP00000005178.5",
"transcript_support_level": 1,
"aa_start": 134,
"aa_end": null,
"aa_length": 411,
"cds_start": 400,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 623,
"cdna_end": null,
"cdna_length": 3601,
"mane_select": "NM_002612.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000005178.6"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000886049.1",
"protein_id": "ENSP00000556108.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 411,
"cds_start": 400,
"cds_end": null,
"cds_length": 1236,
"cdna_start": 925,
"cdna_end": null,
"cdna_length": 3903,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886049.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.394A>G",
"hgvs_p": "p.Met132Val",
"transcript": "ENST00000886050.1",
"protein_id": "ENSP00000556109.1",
"transcript_support_level": null,
"aa_start": 132,
"aa_end": null,
"aa_length": 409,
"cds_start": 394,
"cds_end": null,
"cds_length": 1230,
"cdna_start": 623,
"cdna_end": null,
"cdna_length": 3603,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886050.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000886051.1",
"protein_id": "ENSP00000556110.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 407,
"cds_start": 400,
"cds_end": null,
"cds_length": 1224,
"cdna_start": 629,
"cdna_end": null,
"cdna_length": 3595,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000886051.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000943773.1",
"protein_id": "ENSP00000613832.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 398,
"cds_start": 400,
"cds_end": null,
"cds_length": 1197,
"cdna_start": 531,
"cdna_end": null,
"cdna_length": 3467,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943773.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000943769.1",
"protein_id": "ENSP00000613828.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 393,
"cds_start": 400,
"cds_end": null,
"cds_length": 1182,
"cdna_start": 662,
"cdna_end": null,
"cdna_length": 3582,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943769.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000943768.1",
"protein_id": "ENSP00000613827.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 385,
"cds_start": 400,
"cds_end": null,
"cds_length": 1158,
"cdna_start": 659,
"cdna_end": null,
"cdna_length": 3559,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943768.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000943772.1",
"protein_id": "ENSP00000613831.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 378,
"cds_start": 400,
"cds_end": null,
"cds_length": 1137,
"cdna_start": 530,
"cdna_end": null,
"cdna_length": 3410,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943772.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000943771.1",
"protein_id": "ENSP00000613830.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 374,
"cds_start": 400,
"cds_end": null,
"cds_length": 1125,
"cdna_start": 531,
"cdna_end": null,
"cdna_length": 3398,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943771.1"
},
{
"aa_ref": "M",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val",
"transcript": "ENST00000943770.1",
"protein_id": "ENSP00000613829.1",
"transcript_support_level": null,
"aa_start": 134,
"aa_end": null,
"aa_length": 373,
"cds_start": 400,
"cds_end": null,
"cds_length": 1122,
"cdna_start": 626,
"cdna_end": null,
"cdna_length": 3484,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943770.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "c.131-3173A>G",
"hgvs_p": null,
"transcript": "ENST00000943774.1",
"protein_id": "ENSP00000613833.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 223,
"cds_start": null,
"cds_end": null,
"cds_length": 672,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2823,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943774.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PDK4-AS1",
"gene_hgnc_id": 55767,
"hgvs_c": "n.37-20162T>C",
"hgvs_p": null,
"transcript": "ENST00000665332.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2118,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000665332.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PDK4-AS1",
"gene_hgnc_id": 55767,
"hgvs_c": "n.90-14051T>C",
"hgvs_p": null,
"transcript": "ENST00000667350.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1421,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000667350.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PDK4-AS1",
"gene_hgnc_id": 55767,
"hgvs_c": "n.63-17655T>C",
"hgvs_p": null,
"transcript": "ENST00000669019.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 632,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000669019.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "PDK4-AS1",
"gene_hgnc_id": 55767,
"hgvs_c": "n.545-14051T>C",
"hgvs_p": null,
"transcript": "ENST00000837345.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 759,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000837345.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "PDK4-AS1",
"gene_hgnc_id": 55767,
"hgvs_c": "n.395-14051T>C",
"hgvs_p": null,
"transcript": "ENST00000837346.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 608,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000837346.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"hgvs_c": "n.-129A>G",
"hgvs_p": null,
"transcript": "ENST00000473796.1",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2136,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000473796.1"
}
],
"gene_symbol": "PDK4",
"gene_hgnc_id": 8812,
"dbsnp": "rs144262262",
"frequency_reference_population": 0.0050768377,
"hom_count_reference_population": 88,
"allele_count_reference_population": 8185,
"gnomad_exomes_af": 0.00509402,
"gnomad_genomes_af": 0.00491213,
"gnomad_exomes_ac": 7437,
"gnomad_genomes_ac": 748,
"gnomad_exomes_homalt": 75,
"gnomad_genomes_homalt": 13,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.015191465616226196,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05999999865889549,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.249,
"revel_prediction": "Benign",
"alphamissense_score": 0.178,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.07,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 6.221,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.06,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_002612.4",
"gene_symbol": "PDK4",
"hgnc_id": 8812,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.400A>G",
"hgvs_p": "p.Met134Val"
},
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000665332.1",
"gene_symbol": "PDK4-AS1",
"hgnc_id": 55767,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.37-20162T>C",
"hgvs_p": null
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}